Brooding season, sex ratio, and brood pouch development in the seaweed pipefish, Syngnathus schlegeli, in Otsuchi Bay, Japan

Males of the seaweed pipefish, Syngnathus schlegeli, take care of their eggs in the brood pouch. These pipefish were periodically collected from the shallow seagrass beds in Otsuchi Bay on the Pacific coast of northern Honshu, Japan, from spring to autumn to investigate the basic reproductive ecology. Appearance of the pipefish in the coastal seagrass beds coincided with the initiation of reproduction. The reproductive season was from May to at least October, with its peak in July. A rearing experiment revealed that the brooding period of the male had a negative correlation with water temperature, and it was estimated to last about 1 month in the bay. Almost all males were brooding during the peak of the reproductive season. Although, the brood pouch of most males was either full or devoid of eggs, 6.2% of the males had a partially filled (20%–90%) brood pouch, and multiple clutches were identified in the brood pouch of some males, indicating that the mating system of the pipefish is polygamous, perhaps polygynous. Sex ratio fluctuated among months, and the overall sex ratio tended to be biased to male. Body size of males with an immature brood pouch had a wide range, from 133 to 215 mm standard length (SL). The smallest brooding male was 134 mm SL. Mean SL of brooding males was significantly larger than that of nonbrooding mature males. The number of males with an immature brood pouch was greater at the beginning than later in the reproductive season. The results seem to collectively indicate that the occurrence of a larger proportion of immature males at the onset of the reproductive season may be ascribed to both new recruitment and larger body size at maturation, resulting from the males trading the reproductive effort to somatic growth, perhaps to increase future reproductive success. Received: April 4, 2000 / Revised: September 21, 2000 / Accepted: January 16, 2001     

Spatial differences in breeding success in the pied avocet Recurvirostra avosetta: effects of habitat on hatching success and chick survival

I studied the breeding biology of pied avocets Recurvirostra avosetta in natural habitats (alkaline lakes), and in semi-natural sites (dry fishpond, reconstructed wetlands) in Hungary to relate habitat selection patterns to spatial and temporal variation in breeding success. Colonies were initiated earlier in semi-natural sites than in natural habitats, and earlier on islands than on the mainland. Hatching success was higher on islands than on the mainland, in semi-natural sites than in natural habitats, in colonies of at least 15 pairs than in smaller colonies, and for nests initiated earlier than later within a colony. Fledging success was higher in the wet years (1999–2000) than in the dry year (1998), decreased strongly by season in both habitats and increased with average daily temperature in the first week post-hatch in 1999–2000. Most pairs hatching young in semi-natural sites attempted to lead their chicks to feeding areas in natural habitats, whereas no such movement occurred in the opposite direction. Chick mortality due to predation was high during brood movements and only 23% of the pairs moving their young produced fledglings, compared to 43% for pairs remaining in semi-natural sites and 68% for pairs hatching and rearing young in natural habitats (total n=192 broods). These results suggest that semi-natural sites were more suitable for nesting, whereas natural habitats were more suitable for chick-rearing. The opposing trends in habitat-related breeding success between nesting and chick-rearing suggest sub-optimal habitat selection by Pied Avocets due to an incorrect assessment of the potential for successful reproduction of semi-natural sites, which may thus function as ecological traps.     

Biparental mouthbrooding of the catfish Phyllonemus filinemus in Lake Tanganyika

This article reports biparental mouthbrooding of the bagrid catfish Phyllonemus filinemus in Lake Tanganyika, based on analysis of specimens collected during SCUBA diving. This catfish was nocturnally active, and in the daytime it was concealed singly or in pairs beneath rocks. Within a breeding pair, the male or female alone incubated all the brood in the mouth until the offspring attained 12 mm or so in total length, but thereafter joint mouthbrooding or guarding by both parents took place. Most females of nonbrooding pairs showed high values of gonadosomatic index (GSI), whereas all females of brooding pairs and most single females showed low GSI values. This fact indicated that a pair is formed at a time near the gonadal maturation of the female and separates after the brood is reared. No significant difference in body condition among parents of different reproductive states was observed, which suggested that their condition does not deteriorate markedly as the result of foraging by an off-duty parent. Received: September 16, 2000 / Revised: November 18, 2000 / Accepted: January 23, 2001     

Age and breeding success of a Golden Eagle Aquila chrysaetos population in southeastern Spain

Brood production rate of Grey Partridges Perdix perdix was studied in three areas in Poland in the years 1986–90, by comparing the number of pairs and the number of family coveys after the breeding period. In the study areas, linear permanent nesting cover was mapped and measured. In these areas the brood production rate declined with increasing spring pair density. A positive effect of the occurrence of nesting cover on brood production rate was found. An increase in the population density mostly occurred through occupying parts of the study area avoided earlier, thus presumably less suitable for Partridges. Pairs occupying these less suitable areas, characterized by less abundant nesting cover, had a lower brood production rate, whereas in the preferred areas this rate did not decline with increasing mean population density.     

Brood‐guarding duration in black‐browed albatrosses Thalassarche melanophris: temporal,geographical and individual variation

In birds, the period spent brooding or guarding young chicks is highly variable, but such variation has seldom been studied. Previous single‐year studies of Antarctic petrels Thalassoica antarctica and grey‐headed albatrosses Thalassarche chrysostoma revealed a pronounced seasonal decline in brood‐guarding duration and gave rise to the ‘synchronisation hypothesis’, which suggests that some of the variation in the length of the brood‐guarding stage is related to predictable seasonal changes in the risk of chick predation. We tested the predictions of this and three other hypotheses in a two‐site, four‐year study of the black‐browed albatross T. melanophris. The existence of a pronounced seasonal decline in brood‐guarding duration was apparent at both sites, and in years of contrasting food availability, providing further support for the ‘synchronisation hypothesis’. Alternative explanations for this pattern are that short brood‐guarding periods for late‐hatched chicks result from a seasonal decline in food availability or from the fact that early nesting birds are of higher individual quality. However, these explanations are at odds with the absence of a seasonal decline in early chick growth or in probability of chick survival. Furthermore, adult quality (measured as past reproductive performance) had a weak and inconsistent effect on the duration of brood‐guarding. Weather changes explained some of the variation in brood‐guarding, but there were no differences between regions of contrasting climates. Individual pairs displayed a degree of inter‐annual consistency in brood‐guarding duration and, at least in some years, longer brood‐guarding resulted in higher fledging probability. We speculate that a higher investment in brood‐guarding increases the cost of reproduction, which counteracts other selective pressures that would otherwise lead to longer brood‐guarding durations.     

The effect of partial brood loss on male desertion in a cichlid fish: an experimental test

There is little experimental evidence testing whether currentbrood size and past brood mortality influence mate desertion.In the cichlid Aequidens coeruleopunctatus both parents initiallydefend offspring. In a field study, all experimental broods,irrespective of initial brood size (222.9 ± 60.4, mean± SD), were manipulated to a size of 100 fry. Neitherthe duration nor investment of females in parental care differed between control and brood reduced pairs, even though care seemedcostly. On average, females lost 5.1 ± 4.8% of initialweight while guarding a brood until independence. In contrast,males with experimentally reduced broods guarded fry for significantlyfewer days before deserting their mate than did males fromcontrol pairs with natural-sized broods (20.5 ± 7.5 vs. 14.2 ± 6.2 days). In at least 20% of cases (n = 9/45),the deserting male immediately mated with another female. Maleswith experimentally reduced broods also spent less time guardingfry before deserting and attacked fewer brood predators thandid males with control broods. For broods manipulated to have100 fry, there was a significant negative relationship betweenthe days until male desertion and the proportion of the initialbrood removed. This indicates that male assessment of the futuresuccess of the current brood (hence its reproductive value)is based on past mortality and/or that there is variation amongmales in the expected size of future broods. Both current broodsize and brood size relative to initial brood size are thereforepredictors of male, but not female, parental behavior and matedesertion. Female care may be unaffected by brood reductiondue to limited breeding opportunities and partial compensationfor reduced male care.     

Cooperative nest building and brood care by nestmates and non nestmates in Ropalidia marginata : implications for the evolution of eusociality

In the primitively eusocial wasp, Ropalidia marginata, low levels of intra-colony genetic relatedness, lack of intra-colony kin discrimination and acceptance of young wasps into alien colonies, prompted us to investigate whether or not there exists a cost of such high genetic variability. Freshly eclosed wasps were paired either with their nestmates or with their non nestmates and their performance in nest building and brood care were compared. There was no demonstrable difference between nestmate and non nestmate pairs in terms of success in raising adult offspring, time required for nest initiation, brood developmental period and productivity. There was also no difference in the efficiency of cooperation and division of labour between the nestmate pairs and non nestmate pairs. These results reinforce the idea that the haplodiploidy hypothesis is insufficient to explain the prevalence of worker behaviour in R. marginata and emphasize the importance of factors other than genetic relatedness in the evolution of eusociality. Received: 27 April 1998 / Accepted: 10 July 1998     

Production and costs of nesting attempts in Snow Buntings Plectrophenax nivalis: why do they attempt second broods?

During 1988–1993, pairs of Snow Buntings Plectrophenax nivalis on our study sites in northeast Scotland reared an average of 1.2 broods. Clutch sizes of first and second broods were similar, but partial losses were greater in second broods, leading to a difference of at least 40% in overall nest productivity between successful first and second broods. Over and above this, total nest failure was four times higher in the second broods, and autumn sightings of ringed nestlings from second broods were only a third of those of first-brood nestlings. As a result, second broods produced a mere 10% of future recruits to the breeding population. However, there was also little evidence of costs associated with producing, or attempting to produce, second broods. Young from first broods were not less likely to reach independence if a second brood was attempted, between-year return rates of double-brooded adults were similar to those of single-brooded birds and double-brooded adults did not appear to be less fecund in the following summer. Therefore low costs to the adults of attempting second broods may allow the continuation of a strategy which appears to have only a marginal influence on overall reproductive success in the area studied.     

Multiple-brooding in birds of prey: South African Black Sparrowhawks Accipiter melanoleucus extend the boundaries

Multiple-brooding (raising more than one brood of young in quick succession) occurs infrequently in raptors and is generally restricted to either smaller species with shorter nesting periods, co-operative breeders or species capable of capitalizing on conditions of prolonged food abundance whenever they occur. This paper presents the first recorded cases of multiple-brooding in the Black Sparrowhawk Accipiter melanoleucus from two distinct locales in South Africa. In the Western Cape (Cape Peninsula), four attempts to multiple-brood were recorded in four different years, involving three distinct pairs of birds, and in KwaZulu–Natal (Eshowe), three distinct pairs of Sparrowhawks successfully multiple-brooded on several occasions over a 5-year study period. These results establish the Black Sparrowhawk as one of only two relatively large, monogamous raptor species, and the only specialist bird-eating raptor, in which multiple-brooding has been recorded with any frequency . The species' capacity to thrive in human-modified environments (i.e. alien plantations) and particularly to exploit associated foraging opportunities (e.g. high densities of doves and pigeons in suburban areas) may, at least partly, account for the instances of multiple-brooding reported here. We suggest that biologists be more vigilant for cases of multiple-brooding in raptors, as it is possible that this trait is more common than originally thought and has previously been overlooked.     

Do great tits (Parus major) starve to reproduce?

To test whether nest abandonment is associated with parental health state, reproductive parameters and parental condition indices were examined in relation to brood desertion in great tits. Before desertion, pairs that abandoned their broods in the second half of the nestling period had significantly higher nestling mortality as well as lower average weight of nestlings and entire broods. Independently of brood size, female great tits that deserted their broods on average weighed 1 g (>5%) more than non-deserters. Comparison of metabolic profiles revealed that deserting females were in better nutritional condition (inclined to fat deposition) than non-deserters, which showed symptoms of postresorptive catabolic state, as indicated by a lower level of plasma triglycerides, very low density lipoproteins, and a higher level of free fatty acids and β-hydroxy-butyrate. These results suggest that desertion can be regarded as a reproductive restraint and that non-deserting females invested at least some of their maintenance resources on brood rearing. We found no evidence that desertion or non-desertion was associated with age- or disease-related differences in residual reproductive values. Male condition was not related to brood abandonment, suggesting that desertions were primarily initiated by females. Received: 16 November 1998 / Accepted: 1 February 1999     

Duration and benefits of biparental brood care in the dung beetle Onthophagus vacca (Coleoptera: Scarabaeidae)

Abstract.

• 1 Single males, single females or pairs of dung beetles, Onthophagus vacca, were released on artificial small (100 g) or large (1000 g) dung pats in the laboratory. Emigrating beetles were trapped at 12 h intervals, and the number and size of the brood chambers were recorded after each replicate.
• 2 Emigration of males was delayed if females were present in the same dung pats, whereas emigration times of females were independent of the presence or absence of males.
• 3 A residency of 60 h proved to be a threshold value. Females emigrating before this time did not breed, whereas those emigrating later had built at least two brood chambers.
• 4 Females paired with males built more brood chambers than single females.
• 5 The reproductive success of pairs was not influenced by the size of the dung pats.

     

Pair bond duration influences paternal provisioning and the primary sex ratio of brown thornbill broods

Parents should vary their level of investment in sons and daughters in response to the fitness costs and benefits accrued through male and female offspring. I investigated brood sex ratio biases and parental provisioning behaviour in the brown thornbill, Acanthiza pusilla, a sexually dimorphic Australian passserine. Parents delivered more food to male-biased than female-biased broods. However, factors determining parental provisioning rates differed between the sexes. Female provisioning rates were related to brood sex ratio in both natural and experimental broods with manipulated sex ratios. In contrast, male provisioning rates were not affected by brood sex ratio in either natural or experimental broods. However, males in established pairs provisioned at a higher rate than males in new pairs. Data on the sex ratio of 109 broods suggest that female brown thornbills adjust their primary sex ratio in response to pair bond duration. Females in new pairs produced broods with significantly fewer sons than females in established pairs. This pattern would be beneficial to females if the costs of rearing sons were higher for females in new than established pairs. This may be the case since females in new pairs provisioned experimental all-male broods at elevated rates. The condition of nestlings also tended to decline more in these all-male broods than in other experimental broods. This will have additional fitness consequences because nestling mass influences recruitment in thornbills. Female thornbills may therefore obtain significant fitness benefits from adjusting their brood sex ratio in response to the status of their pair bond. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.     

Effects of Brood Pheromone Modulated Brood Rearing Behaviors on Honey Bee (Apis mellifera L.) Colony Growth

A hallmark of eusociality is cooperative brood care. In most social insect systems brood rearing labor is divided between individuals working in the nest tending the queen and larvae, and foragers collecting food outside the nest. To place brood rearing division of labor within an evolutionary context, it is necessary to understand relationships between individuals in the nest engaged in brood care and colony growth in the honey bee. Here we examined responses of the queen, queen-worker interactions, and nursing behaviors to an increase in the brood rearing stimulus environment using brood pheromone. Colony pairs were derived from a single source and were headed by open-mated sister queens, for a total of four colony pairs. One colony of a pair was treated with 336 μg of brood pheromone, and the other a blank control. Queens in the brood pheromone treated colonies laid significantly more eggs, were fed longer, and were less idle compared to controls. Workers spent significantly more time cleaning cells in pheromone treatments. Increasing the brood rearing stimulus environment with the addition of brood pheromone significantly increased the tempo of brood rearing behaviors by bees working in the nest resulting in a significantly greater amount of brood reared.     

Prudent investment in rearing nestlings in bull-headed shrikes

I investigated seasonal changes in the relationships between brood size, body mass of nestlings and body mass of parents of the bull-headed shrike, Lanius bucephalus, in Ishikari, northern Japan. When the broods were 12days old, the body mass of the heaviest nestling in a brood did not differ among brood sizes, or throughout the season. However, the body mass of the lightest nestlings in a brood was different among brood sizes. The body mass of the lightest nestling in five- and six-nestling broods decreased throughout the season. The lightest nestling in four-nestling broods, and the lightest and the second lightest nestlings in five-nestling broods, were significantly lighter than the heaviest nestling in broods of this size. It is likely that pairs with six nestlings at 12days old can feed at least five of these nestlings enough to ensure their survival . The standardized body mass of parents (SBM), which was defined as the body mass divided by the length of the tarsus, did not differ among brood sizes, or throughout the season. It is possible that the relationship between the constancy of the SBM and the seasonal decline in the body mass of nestlings indicates that bull-headed shrikes have a limit to their parental efforts.     

The effect of beaver facilitation on Common Teal: pairs and broods respond differently at the patch and landscape scales

Avian species respond to ecological variability at a range of spatial scales and according to life history stage. Beaver dams create wetland systems for waterbirds that are utilized throughout different stages of the breeding season. We studied how beaver‐induced variability affected mobile pairs and more sedentary broods along with the production of Common Teal Anas crecca at the patch and landscape scale on their breeding grounds. Beavers Castor spp. are ecosystem engineers that enhance waterfowl habitats by impeding water flow and creating temporary flooding. Two landscapes in southern Finland with (Evo) and without (Nuuksio) American Beavers Castor canadensis were used in this study. To investigate the patch‐scale effect, pair and brood densities along with brood production were first compared at beaver‐occupied lakes and non‐beaver lakes in the beaver landscape. Annual pair and brood densities/km shoreline and brood production were compared between beaver and non‐beaver landscapes. Facilitative effects of beaver activity were manifest on brood density at both patch and landscape scales: these were over 90% and 60% higher in beaver patches and landscapes, respectively. An effect of beaver presence on pair density was only seen at the landscape level. Pair density did not strongly affect brood production, as shown earlier for relatively mildly density‐dependent Teal populations. Because the extent of beaver flooding was a crucial factor affecting annual Teal production in the study area, we infer beaver activity has consequences for the local Teal population. Ecosystem engineering by the beaver could therefore be considered a restoration tool in areas where waterfowl are in need of high‐quality habitats.     

The social system of the Pale Chanting Goshawk Melierax canorus; monogamy v polyandry and delayed dispersal

The social organization and reproductive strategy of the Pale Chanting Goshawk Melierax canorus were investigated in four southern African study areas. Territories supporting adults additional to the breeding pair were observed in two study areas. Within one of these areas, these additional adults were either non-breeders staying in their natal territory but actively excluded from the nesting area during the breeding season or a male cobreeder participating fully in reproductive activities with the breeding pair. Polyandrous trios were, however, observed in only one vegetation type in this area, Broken Veld. The annual number of offspring fledged per group did not differ significantly between vegetation types nor between polyandrous trios and monogamous pairs within Broken Veld. Pale Chanting Goshawks lay predominantly two-egg clutches. In 2 out of 5 years, breeding groups succeeded in laying, hatching and even fledging a second brood of young after successfully fledging their first brood. Double brooding occurred more frequently in Broken Veld and most frequently in polyandrous trios in this vegetation type. To accommodate their relatively long breeding cycle (>115 days) in this temperate study area with its limiting summer breeding period, double-brooding Pale Chanting Goshawks laid the first clutch in midwinter and the second, on average, 24 days after the offspring from the first brood left the nest.     

Density-dependent decline of breeding success in an introduced, increasing mute swan Cygus olor population

An increasing population of the mute swan Cygnus olor , was studied from its very establishment in 1976 until 1998. As the number of pairs increased, there was a decline in all production parameters, including the average number of clutches per pair, the average number of broods per clutch, and the average number of fledged young per brood. In a multiple regression analysis covering the whole breeding season, the number of pairs and the average number of clutches per pair explained 71% of the variation in the average number of fledglings per pair. During the brood season, the average number of fledglings per brood was an additionally important parameter in explaining fledgling production. Habitat quality seemed to affect breeding: in places occupied earlier more cygnets fledged from a clutch than in habitats inhabited later. The decreased production of young very likely reflects density-dependent effects on reproduction. This density dependence seems to operate on the breeding grounds, since winter harshness did not affect breeding success. Density-dependent processes started acting already when pairs were beginning to nest, and continued during the brood period. Density dependence has apparently not been detected at the pair stage in earlier studies of bird populations.     

Reproduction of Varroa destructor in worker brood of Africanized honey bees (Apis mellifera)

Reproduction and population growth of Varroa destructor was studied in ten naturally infested, Africanized honeybee (AHB) (Apis mellifera) colonies in Yucatan, Mexico. Between February 1997 and January 1998 monthly records of the amount of pollen, honey, sealed worker and drone brood were recorded. In addition, mite infestation levels of adult bees and worker brood and the fecundity of the mites reproducing in worker cells were determined. The mean number of sealed worker brood cells (10,070 ± 1,790) remained fairly constant over the experimental period in each colony. However, the presence and amount of sealed drone brood was very variable. One colony had drone brood for 10 months and another for only 1 month. Both the mean infestation level of worker brood (18.1 ± 8.4%) and adult bees (3.5 ± 1.3%) remained fairly constant over the study period and did not increase rapidly as is normally observed in European honey bees. In fact, the estimated mean number of mites fell from 3,500 in February 1997 to 2,380 in January 1998. In May 2000 the mean mite population in the study colonies was still only 1,821 mites. The fertility level of mites in this study was much higher (83–96%) than in AHB in Brazil(25–57%), and similar to that found in EHB (76–94%). Mite fertility remained high throughout the entire study and was not influenced by the amount of pollen, honey or worker brood in the colonies. This revised version was published online in July 2006 with corrections to the Cover Date.     

Lasioglossum (Dialictus) tenax (Sandhouse) (Hymenoptera: Halictidae) as a solitary sweat bee

Summary Nine nests ofLasioglossum (Dialictus) tenax were excavated near Calgary, Alberta, Canada over a time period encompassing the entire brood production period in 1988. Each nest contained a maximum of one active adult female, nest productivity peaked in mid July, protandry was noted and no significant size difference between foundresses and the earlier emerging females was detected. These data suggest that this species is solitary. These results are compared with data for the sympatrically nesting eusocial speciesL. (D.) laevissimum.